M. Weigell-Weber

发表

[Hereditary hearing loss due to mutations in the connexin-26 gene].

A. Schinzel, M. Hergersberg, M. Weigell-Weber, 2000, Schweizerische medizinische Wochenschrift.

Mcleod syndrome: A novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings

K. Hess, H. Alkadhi, S. Kneifel, 2001, Annals of neurology.

DNA analysis of Huntington’s disease

O. Riess, C. Zühlke, G. von Beust, 1999, Neurology.

Psychiatric symptoms and CAG expansion in Huntington's disease.

R. Spiegel, W. Schmid, M. Weigell-Weber, 1996, American journal of medical genetics.

Genomewide homozygosity mapping and molecular analysis of a candidate gene located on 22q13 (fibulin-1) in a previously undescribed vitreoretinal dystrophy.

L. Sandkuijl, E. Messmer, M. Hergersberg, 2003, Archives of ophthalmology.

A NOVEL COMPLEX MUTATION EVENT IN THE PERIPHERIN/RDS GENE IN A FAMILY WITH RETINAL PATTERN DYSTROPHY

B. Pajic, E. R. Büchi, R. Spiegel, 2006, Retina.

Striatal glucose metabolism and dopamine D2 receptor binding in asymptomatic gene carriers and patients with Huntington's disease.

P Boesiger, D Meier, A Weindl, 1996, Brain : a journal of neurology.

Codons 837 and 838 in the retinal guanylate cyclase gene on chromosome 17p: hot spots for mutations in autosomal dominant cone-rod dystrophy?

A. Schinzel, S. Fokstuen, M. Hergersberg, 2000, Archives of ophthalmology.

Genetic heterogeneity in autosomal dominant pattern dystrophy of the retina.

E. R. Büchi, R. Spiegel, M. Weigell-Weber, 1996, Molecular vision.

DNA analysis of Huntington’s disease

G. Schluter, C. Zühlke, D. Morris-Rosendahl, 1999, Neurology.

Clinical description and exclusion of candidate genes in a novel autosomal recessively inherited vitreoretinal dystrophy.

E. Messmer, M. Hergersberg, D. Kotzot, 2003, A M A Archives of Ophthalmology.